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FDA 510(k) Applications Submitted by DAVID A PUTZ
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990788
03/10/1999
AD-TECH'S FORAMEN OVALE ELECTRODE
AD-TECH MEDICAL INSTRUMENT CORP.
K964644
10/31/1996
AD-TECH'S DEPTH ELECTRODE
AD-TECH MEDICAL INSTRUMENT CORP.
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